Abstract Background Patients with congenital afibrinogenemia suffer from spontaneous recurrent severe bleeding. While fibrinogen concentrates are known to effectively treat bleeding episodes, thrombotic complications often occur upon replacement therapy, rendering clinical management highly challenging. Case Presentation We hereby report a case of combined afibrinogenemia and congenital antithrombin deficiency manifested by recurrent life-threatening bleeding, as well as spontaneous severe arterial occlusion, such as acute coronary syndrome and stroke, and venous thromboses like pulmonary embolism. Secondary fibrinogen prophylaxis is recommended following any initial life-threatening bleeding episode in patients with afibrinogenemia, yet th...
This review of published studies was conducted to derive data on patients with congenital fibrinogen...
Congenital fibrinogen disorders are rare pathologies of the hemostasis, comprising quantitative (afi...
Thrombosis has been occasionally described in congenital FVII de\ufb01ciency. This report deals with...
Although congenital afibrinogenemia is a rare autosomal recessive bleeding disorder, it can be more ...
Congenital afibrinogenemia (CA) is a disease characterized by a complex pathophysiology, involving b...
Frequent arterial and venous thromboembolism in patients with congenital afibrinogenaemia (CA) is ne...
Frequent arterial and venous thromboembolism in patients with congenital afibrinogenaemia (CA) is ne...
Congenital fibrinogen deficiency is a rare bleeding disorder, affecting either the quantity (afibrin...
Fibrinogen is a complex protein playing a major role in coagulation. Congenital afibrinogenemia, cha...
Congenital fibrinogen disorders are rare diseases affecting either the quantity (afibrinogenemia and...
Congenital afibrinogenaemia (CA), is a rare inherited bleeding disorder characterised by complete de...
The authors present the case of a 27-year-old patient who suffered from spontaneous bleeding during ...
Background-Coagulation disorders can cause intracerebral bleeding that may be difficult to detect si...
Knowledge of the spectrum of symptoms in patients with inherited afibrinogenaemia is limited by the ...
Congenital deficiency of plasma fibrinogen is a hereditary bleeding disorder with an autosomal reces...
This review of published studies was conducted to derive data on patients with congenital fibrinogen...
Congenital fibrinogen disorders are rare pathologies of the hemostasis, comprising quantitative (afi...
Thrombosis has been occasionally described in congenital FVII de\ufb01ciency. This report deals with...
Although congenital afibrinogenemia is a rare autosomal recessive bleeding disorder, it can be more ...
Congenital afibrinogenemia (CA) is a disease characterized by a complex pathophysiology, involving b...
Frequent arterial and venous thromboembolism in patients with congenital afibrinogenaemia (CA) is ne...
Frequent arterial and venous thromboembolism in patients with congenital afibrinogenaemia (CA) is ne...
Congenital fibrinogen deficiency is a rare bleeding disorder, affecting either the quantity (afibrin...
Fibrinogen is a complex protein playing a major role in coagulation. Congenital afibrinogenemia, cha...
Congenital fibrinogen disorders are rare diseases affecting either the quantity (afibrinogenemia and...
Congenital afibrinogenaemia (CA), is a rare inherited bleeding disorder characterised by complete de...
The authors present the case of a 27-year-old patient who suffered from spontaneous bleeding during ...
Background-Coagulation disorders can cause intracerebral bleeding that may be difficult to detect si...
Knowledge of the spectrum of symptoms in patients with inherited afibrinogenaemia is limited by the ...
Congenital deficiency of plasma fibrinogen is a hereditary bleeding disorder with an autosomal reces...
This review of published studies was conducted to derive data on patients with congenital fibrinogen...
Congenital fibrinogen disorders are rare pathologies of the hemostasis, comprising quantitative (afi...
Thrombosis has been occasionally described in congenital FVII de\ufb01ciency. This report deals with...